They're not the sharpest people - babies. So, you must be everything to them.
Families with disabled children are praying for their kids to die before them because they have no support systems. They are very scared about who will take care of their kids and how their kids will have a dignified life after they die.
I’ve got my own Medicare plan. I’ve got an intern for a son-in-law.
Few years ago when I visited a palliative care centre in Chennai for the first time, it completely moved me. It's an emotionally draining experience. I saw and met patients who were abandoned by their families, and there is complete sense of hopelessness. Ever since, I have been a supporter for the need for funding and awareness of palliative care.
With the right care at the right time, a huge number of people could stay independent much longer, with a higher quality of life.
You know, some people think since I can't move I am a vegetable. Wrong. Just picture yourself as you are, just always sitting down and if you need something a hot babe takes care of you. I am exaggerating a little, but this is how I see it.
I don't know a great deal about Alzheimer's - just what it does.
I've been supporting Help for Heroes for many years - I actually rode in their first-ever official fundraiser back in 2008. I have witnessed the great work that Help for Heroes do to support those who have suffered life-changing injuries and illnesses, and I want to do all I can to help raise as much as possible.
Military caregivers play an essential role in the recovery process of our veterans and are more than deserving of our support.
There are many women with children under five who want to work and who lack affordable, high-quality child care.
There are so many people getting dementia. It is like an epidemic now. It is a terrible disease because once you get it, your life changes completely.
I can relate to a guy who stays home and does it for his family and friends.
I have recently been told that I am one of the millions of Americans who will be afflicted with Alzheimer's Disease. . .. I now begin the journey that will lead me into the sunset of my life. I know that for America there will always be a bright dawn ahead.
With Alzheimer's patients, you have to be very careful what you say when you're looking at them over their bed. Because once in a while, they understand it.
Family caregiving has become a predictable crisis. Americans are living longer and longer but dying slower and slower.
My mother passed away of complications of dementia. As you get older, it really makes you realize how many people are touched by this disease.
One of the great changes wrought by the increased public awareness of Alzheimer's - and thank you, Nancy Reagan, you wonderful tough old dame, you - is that people in the early stages of the disease are now speaking out while they still have the capacity to do so.
I can't get people to understand how important the Alzheimer's fight is to me.
There are only four kinds of people in the world - those who have been caregivers, those who are caregivers, those who will be caregivers and those who will need caregivers.
Nearly every American will encounter the need for long-term care.
In 2011, my wife, Courtney, and I, with my amazing mother and sister, opened the Nantz National Alzheimer Center at Houston Methodist Hospital.
Workplaces need to respond to the reality of family life in the 21st century, and allowing employees to have seven sick days a year is a bare minimum, the fact that the United States is one of just a handful of countries that does not require paid family or sick leave is nothing short of shameful.
Dementia is not exclusively a problem of the developed world.
My mother got down sick in 53 and she lived with me, an invalid, until she passed away in 1961. And during the time she was staying with me sometime I would be worked so hard I couldn't sleep at night.
In 2009, I served as AARP's Ambassador of Caregiving. With a producer and cameraman, I traveled the country for months, interviewing hundreds of caregivers.
